ClinVar Miner

Submissions for variant NM_017950.4(CCDC40):c.677-3del

dbSNP: rs886038641
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000241972 SCV000313113 likely benign not specified criteria provided, single submitter clinical testing
Invitae RCV003535674 SCV004280611 benign Primary ciliary dyskinesia 2023-05-18 criteria provided, single submitter clinical testing

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